- Type
- Assignment
- Course
- BIF401 Bioinformatics I
- Size
- PDF 460 KB
- Updated
- 23 Oct 2026
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ہر طالب علم کو انسانوں کا مختلف پروٹین چننا ہوگا اور پھر یہ تمام عمل شروع سے ا ٓٓٓ ٓ خر
- Go to the NCBI database at
- In the search bar, type the name of the protein you're interested in. For
example, let's say we're interested in the protein " Hemoglobin, alpha 1".
Type that into the search bar and hit enter.
- Click on the first result under the " Protein" category.
- On this page, you will find the information you need: the sequence is
displayed under the "SEQUENCE" section, the accession number is listed
at the top of the page, the sequence length is displayed next to the
sequence, and the function of the protein is usually described in the
" General protein information" section.
a) Protein Selected
Hemoglobin Alpha 1
>AAB59408.1 hemoglobin alpha 1 [Homo sapiens] MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNA VAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSK YR
d)Sequence Length :
e)Functions of Selected Protein (Hemoglobin Alpha1)
1. Oxygen Binding: Hemoglobin Alpha 1 combines with three other
subunits (two Beta and two Alpha) to form a functional hemoglobin molecule.
It binds and carries oxygen from the lungs to tissues throughout the body,
ensuring an adequate oxygen supply for cellular respiration.
2. Carbon Dioxide Transport: Hemoglobin Alpha 1 also assists in carrying
carbon dioxide, a waste product of cellular metabolism, from the tissues back
to the lungs, where it is exhaled.
3. pH Regulation: Hemoglobin Alpha 1 helps maintain the pH balance in
the blood by binding to hydrogen ions (H+). This buffering capacity helps
prevent significant changes in blood pH, contributing to overall physiological
homeostasis.
4. Allosteric Regulation: Hemoglobin Alpha 1 participates in allosteric
interactions with other hemoglobin subunits, affecting its affinity for oxygen.
This allows hemoglobin to adapt to varying oxygen concentrations, facilitating
efficient oxygen loading and unloading in different tissues.
5. Genetic Disorders: Mutations in the Hemoglobin Alpha 1 gene can result
in hemoglobinopathies, such as alpha-thalassemia or Hb Bart's hydrops fetalis
syndrome, which affect the production or structure of hemoglobin, leading to
various health complications.
- Paste the protein sequences of the same gene from 5 different species into
the box. You can obtain these sequences from the NCBI database, just like
you did in Step 1.
- Select " Phylip" as the output format.
- Click the " Run" button.
- Once the results load, you can capture them for your document.
clustalw.phy
XP_0543092 MVLSPADKTN VKTAWGKVGA HAGDYGAEAL ERMFLSFPTT KTYFPHFDLS
Q9. TS35.2_1 MVLSPADKTN VKAAWGKVGA HAGDYGAEAL ERMFLSFPTT KTYFPHFDLS
XP_0040569 MVLSPADKTN VKAAWGKVGA HAGDYGAEAL ERMFLSFPTT KTYFPHFDLS HDS1036830 MVLSPADKTN VKAAWGKVGA HAGEYGAEAL ERMFLSFPTT KTYFPHFDLS
HCS8797820 MVLSPADKTN VKAAWGKVGA HAGEYGAEAL ERMFLSFPTT KTYFPHFDLS XP_0103801 MVLSPADKTN VKAAWGKVGG HGGEYGAEAL ERMFLSFPTT KTYFPHFDLS HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK
HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK HGSAQVKGHG KKVADALTNA VAHVDDMPNA LSALSDLHAH KLRVDPVNFK
LLSHCLLVTL AAHLPAEFTP AVHASLDKFL ASVSTVLTSK YR LLSHCLLVTL AAHHPAEFTP AVHASLDKFL ASVSTVLTSK YR LLSHCLLVTL AAHLPAEFTP AVHASLDKFL ASVSTVLTSK YR LLSHCLLVTL AAHLPAEFTP AVHASLDKFL ASVSTVLTSK -- LLSHCLLVTL AAHLPAEFTP AVHASLDKFL ASVSTVLTSK -- LLSHCLLVTL AAHLPAEFTP AVHASLDKFL ASVSTVLTSK YR
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